Variant report

Variant	esv2830377
Chromosome Location	chrX:75525310-76337197
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1937)
CpG islands
(count:1040)
Chromatin interactive
region (count:12)
LncRNA
region (count:31)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1937 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:76308187-76308500	HepG2	liver:	n/a	n/a
2	ATF2	chrX:76152081-76152335	GM12878	blood:	n/a	n/a
3	ATF2	chrX:76151955-76152368	GM12878	blood:	n/a	n/a
4	ATF2	chrX:76192463-76192772	GM12878	blood:	n/a	n/a
5	BACH1	chrX:76036215-76036417	K562	blood:	n/a	n/a
6	BACH1	chrX:76235036-76235745	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chrX:76197900-76198349	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chrX:75654787-75655105	H1-hESC	embryonic stem cell:	n/a	chrX:75654921-75654935
9	BATF	chrX:76224411-76224630	GM12878	blood:	n/a	chrX:76224553-76224564
10	BATF	chrX:76271981-76272136	GM12878	blood:	n/a	n/a
11	BATF	chrX:75877918-75878160	GM12878	blood:	n/a	n/a
12	BHLHE40	chrX:76180553-76180590	GM12878	blood:	n/a	n/a
13	BHLHE40	chrX:76308184-76308632	HepG2	liver:	n/a	n/a
14	BHLHE40	chrX:76235184-76235740	HepG2	liver:	n/a	chrX:76235605-76235621
15	BHLHE40	chrX:75901969-75901984	GM12878	blood:	n/a	n/a
16	CBX3	chrX:75775702-75775978	K562	blood:	n/a	n/a
17	CEBPB	chrX:76023198-76023471	IMR90	lung:	n/a	chrX:76023327-76023338
18	CEBPB	chrX:76041127-76041312	K562	blood:	n/a	n/a
19	CEBPB	chrX:76273946-76274569	IMR90	lung:	n/a	n/a
20	CEBPB	chrX:76142525-76142852	A549	lung:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
21	CEBPB	chrX:76142635-76142827	MCF-7	breast:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
22	CEBPB	chrX:76265879-76266180	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chrX:76308399-76308504	HepG2	liver:	n/a	n/a
24	CEBPB	chrX:76023128-76023501	MCF-7	breast:	n/a	chrX:76023327-76023338
25	CEBPB	chrX:76142548-76142909	IMR90	lung:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
26	CEBPB	chrX:76142547-76142899	MCF-7	breast:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
27	CEBPB	chrX:76142546-76142909	HepG2	liver:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
28	CEBPB	chrX:76035776-76036091	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:76138554-76139001	Hela-S3	cervix:	n/a	chrX:76138949-76138960 chrX:76138681-76138694
30	CEBPB	chrX:76023146-76023536	Hela-S3	cervix:	n/a	chrX:76023327-76023338
31	CEBPB	chrX:76127068-76127235	K562	blood:	n/a	chrX:76127191-76127202
32	CEBPB	chrX:75568039-75568326	IMR90	lung:	n/a	n/a
33	CEBPB	chrX:76127054-76127370	HepG2	liver:	n/a	chrX:76127191-76127202
34	CEBPB	chrX:75682115-75682328	K562	blood:	n/a	n/a
35	CEBPB	chrX:75568080-75568294	A549	lung:	n/a	n/a
36	CEBPB	chrX:76142558-76142904	H1-hESC	embryonic stem cell:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
37	CEBPB	chrX:76023166-76023512	A549	lung:	n/a	chrX:76023327-76023338
38	CEBPB	chrX:76023101-76023544	A549	lung:	n/a	chrX:76023327-76023338
39	CEBPB	chrX:76273946-76274365	A549	lung:	n/a	n/a
40	CEBPB	chrX:76296445-76296718	HepG2	liver:	n/a	chrX:76296587-76296598
41	CEBPB	chrX:76023246-76023372	K562	blood:	n/a	chrX:76023327-76023338
42	CEBPB	chrX:76296467-76296686	A549	lung:	n/a	chrX:76296587-76296598
43	CEBPB	chrX:76033633-76033833	A549	lung:	n/a	n/a
44	CEBPB	chrX:76138558-76139038	HepG2	liver:	n/a	chrX:76138949-76138960 chrX:76138681-76138694
45	CEBPB	chrX:75682076-75682373	IMR90	lung:	n/a	n/a
46	CEBPB	chrX:76137566-76137851	HepG2	liver:	n/a	n/a
47	CEBPB	chrX:75568082-75568284	K562	blood:	n/a	n/a
48	CEBPB	chrX:76142542-76142920	K562	blood:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
49	CEBPB	chrX:76308048-76308667	HepG2	liver:	n/a	n/a
50	CEBPB	chrX:76127037-76127262	IMR90	lung:	n/a	chrX:76127191-76127202

(count:1040 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:75647595-75647645	HRE	kidney:	n/a
2	chrX:75648884-75648934	PANC-1	pancreas:	n/a
3	chrX:75648455-75648505	GM12878	blood:	n/a
4	chrX:75647595-75647645	HRE	kidney:	n/a
5	chrX:75648884-75648934	PANC-1	pancreas:	n/a
6	chrX:75648455-75648505	GM12878	blood:	n/a
7	chrX:75649532-75649582	AG10803	skin:	n/a
8	chrX:75648802-75648852	AG09309	skin:	n/a
9	chrX:75648083-75648133	ECC-1	luminal epithelium:	n/a
10	chrX:76140313-76140363	HNPCEpiC	eye:	n/a
11	chrX:75648019-75648069	MCF-7	breast:	n/a
12	chrX:76198371-76198421	ECC-1	luminal epithelium:	n/a
13	chrX:75648222-75648272	K562	blood:	n/a
14	chrX:75647436-75647486	SK-N-MC	brain:	n/a
15	chrX:75648992-75649042	PFSK-1	brain:	n/a
16	chrX:75647859-75647909	NHBE	bronchial:	n/a
17	chrX:75648222-75648272	ECC-1	luminal epithelium:	n/a
18	chrX:75648992-75649042	AG04449	skin:	fetal
19	chrX:75648216-75648266	NB4	blood:	n/a
20	chrX:75648019-75648069	LNCaP	prostate:	n/a
21	chrX:75647859-75647909	ovcar-3	ovarian:	n/a
22	chrX:75649532-75649582	HepG2	liver:	n/a
23	chrX:75649532-75649582	U87	brain:	n/a
24	chrX:75649532-75649582	SK-N-MC	brain:	n/a
25	chrX:75647595-75647645	AoSMC	blood vessel:	n/a
26	chrX:75647859-75647909	HRCEpiC	kidney:	n/a
27	chrX:75649367-75649417	NHBE	bronchial:	n/a
28	chrX:75648083-75648133	HCF	heart:	n/a
29	chrX:75648019-75648069	HNPCEpiC	eye:	n/a
30	chrX:76140313-76140363	MCF-7	breast:	n/a
31	chrX:75648802-75648852	Hepatocyte	liver:	n/a
32	chrX:75648083-75648133	PFSK-1	brain:	n/a
33	chrX:75647859-75647909	SKMC	muscle:	n/a
34	chrX:75649367-75649417	HIPEpiC	eye:	n/a
35	chrX:75649532-75649582	HCF	heart:	n/a
36	chrX:75648216-75648266	GM12891	blood:	n/a
37	chrX:75648216-75648266	HPAEpiC	pulmonary alveolar:	n/a
38	chrX:75648992-75649042	HUVEC	blood vessel:	n/a
39	chrX:75649367-75649417	HepG2	liver:	n/a
40	chrX:75648083-75648133	BJ	skin:	n/a
41	chrX:75647436-75647486	HRCEpiC	kidney:	n/a
42	chrX:75648802-75648852	AG04450	lung:	fetal
43	chrX:76198371-76198421	HUVEC	blood vessel:	n/a
44	chrX:75647436-75647486	HMEC	breast:	n/a
45	chrX:75649761-75649811	HEEpiC	esophagus:	n/a
46	chrX:76140313-76140363	AG09309	skin:	n/a
47	chrX:75649761-75649811	HCPEpiC	choroid plexus:	n/a
48	chrX:75649532-75649582	HMEC	breast:	n/a
49	chrX:75648083-75648133	HAEpiC	amniotic membrane:	n/a
50	chrX:75648455-75648505	HCM	heart:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:77165670..77166520-chrX:75928241..75929119,2	NB4	blood:
2	chrX:75912856..75913411-chrX:76635366..76635882,2	MCF-7	breast:
3	chr4:41992370..41992871-chrX:76089886..76090386,2	Hela-S3	cervix:
4	chrX:76232252..76234019-chrX:76241315..76243739,2	K562	blood:
5	chr4:190533382..190535450-chrX:76020791..76023770,2	MCF-7	breast:
6	chrX:76278562..76281311-chrX:76283274..76285842,2	K562	blood:
7	chrX:75499134..75500029-chrX:75674724..75676050,4	MCF-7	breast:
8	chr1:149214888..149215551-chrX:76308420..76309419,2	MCF-7	breast:
9	chr20:52749844..52752672-chrX:76227808..76229967,2	MCF-7	breast:
10	chr1:149214438..149216121-chrX:76307420..76308940,2	MCF-7	breast:
11	chrX:76232252..76234019-chrX:76241315..76243739,2	K562	blood:
12	chrX:76278562..76281311-chrX:76283274..76285842,2	K562	blood:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATRX-2	chrX:75794602-75795113	ucscGeneNc_uc010nlv_1
2	lnc-ATRX-1	chrX:75878198-75878709	NONHSAT137681
3	lnc-ATRX-1	chrX:75878198-75878709	NR_110401
4	lnc-ATRX-1	chrX:76234652-76234957	NR_110406
5	lnc-MAGEE2-5	chrX:75875899-75876960	NONHSAT137680
6	lnc-ATRX-1	chrX:75913366-75913486	NONHSAT137681
7	lnc-ATRX-1	chrX:76234652-76234957	NR_110400
8	lnc-ATRX-1	chrX:75878198-75878709	NR_110404
9	lnc-ATRX-1	chrX:76234652-76234957	NR_110401
10	lnc-ATRX-2	chrX:76151043-76151348	ucscGeneNc_uc010nlv_1
11	lnc-ATRX-2	chrX:76144092-76144196	ucscGeneNc_uc010nlv_1
12	lnc-ATRX-1	chrX:75878903-75879069	NR_110401
13	lnc-ATRX-1	chrX:76234652-76234957	NR_110403
14	lnc-CXorf26-6	chrX:75651475-75651742	NONHSAT137678
15	lnc-ATRX-1	chrX:76227701-76227805	NR_110401
16	lnc-ATRX-1	chrX:76001608-76001717	NR_110405
17	lnc-ATRX-1	chrX:75878198-75878709	NR_110403
18	lnc-ATRX-1	chrX:75878903-75879069	NR_110400
19	lnc-ATRX-1	chrX:75913366-75913486	NR_110400
20	lnc-ATRX-1	chrX:75878198-75878709	NR_110405
21	lnc-ATRX-1	chrX:75913366-75913486	NR_110403
22	lnc-ATRX-1	chrX:76227701-76227805	NR_110406
23	lnc-ATRX-2	chrX:75829770-75829890	ucscGeneNc_uc010nlv_1
24	lnc-ATRX-1	chrX:75878198-75878709	NR_110400
25	lnc-ATRX-1	chrX:76234652-76234957	NR_110404
26	lnc-ATRX-1	chrX:76058235-76058317	NR_110403
27	lnc-ATRX-1	chrX:75878198-75878709	NR_110406
28	lnc-ATRX-1	chrX:76234652-76234957	NONHSAT137681
29	lnc-ATRX-1	chrX:75878903-75879069	NR_110404
30	lnc-ATRX-1	chrX:76234652-76234957	NR_110405
31	lnc-ATRX-1	chrX:76227701-76227805	NONHSAT137681

miRNA name	Chromosome Location	mirBase accession
hsa-miR-325	chrX:76225889-76225911	MIMAT0000771
hsa-miR-384	chrX:76139710-76139729	MIMAT0001075

No data

Variant related genes	Relation type
RNA5SP509	TF binding region
MIR325	TF binding region
MAGEE1	TF binding region
ENSG00000235447	TF binding region
RNA5SP508	TF binding region
LDHBP2	TF binding region
RNA5SP509	CpG island
MIR325	CpG island
MAGEE1	CpG island
ENSG00000235447	CpG island
RNA5SP508	CpG island
LDHBP2	CpG island
ENSG00000014824	chromatin interactions
ENSG00000252826	chromatin interactions
NTRK3	Mature miRNA region

Extended variants
information (count: 2257 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:2257 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192817026	chrX:75539102-75539103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs372338686	chrX:75539385-75539386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184896027	chrX:75539444-75539445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs112956824	chrX:75539556-75539557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs68045207	chrX:75539575-75539576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369680994	chrX:75539687-75539688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12011114	chrX:75539692-75539693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188160729	chrX:75539700-75539701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs67194719	chrX:75539714-75539715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140140189	chrX:75539778-75539779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192893241	chrX:75539784-75539785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183740831	chrX:75539790-75539791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs188072899	chrX:75539834-75539835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs181954870	chrX:75539843-75539844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs147110227	chrX:75539940-75539941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs66814291	chrX:75540092-75540093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143853098	chrX:75540161-75540162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190276791	chrX:75540192-75540193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs146391433	chrX:75540196-75540197	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs181490219	chrX:75540257-75540258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139436187	chrX:75540261-75540262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372778643	chrX:75540275-75540276	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs186966766	chrX:75540284-75540285	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377442103	chrX:75540291-75540292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs5982085	chrX:75540299-75540300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs191354416	chrX:75540352-75540353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs68178710	chrX:75540364-75540365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149155858	chrX:75540435-75540436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374621130	chrX:75540446-75540447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181210392	chrX:75540451-75540452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377723697	chrX:75540493-75540494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs5981449	chrX:75540520-75540521	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs5981450	chrX:75540525-75540526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75939001	chrX:75548448-75548449	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs368816719	chrX:75548484-75548485	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs368235534	chrX:75548510-75548511	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs201120077	chrX:75548541-75548542	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs186863109	chrX:75548544-75548545	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs12833978	chrX:75548635-75548636	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs375232909	chrX:75548662-75548663	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs12833537	chrX:75548718-75548719	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs371418395	chrX:75548754-75548755	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs190368620	chrX:75548805-75548806	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs182559609	chrX:75548849-75548850	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs61495096	chrX:75548853-75548854	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs372680459	chrX:75548859-75548860	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs200708498	chrX:75548900-75548901	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs373340485	chrX:75548924-75548925	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs375221066	chrX:75548933-75548934	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs369477947	chrX:75549063-75549064	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Lujan-Fryns syndrom	21572526	CNVD
Opitz-Kaveggia syndrome	21572526	CNVD
Cerebellar atrophy	21569638	CNVD
X-linked sideroblastic anemia	21569638	CNVD
Mental retardation	21572526	CNVD
ATR-X Syndrome	22470819	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Premature ovarian failure	20952765	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:75539000-75539400	Enhancers	Dnd41	blood
2	chrX:75539000-75539600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
3	chrX:75539000-75540000	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chrX:75539000-75540400	Enhancers	Primary T cells fromperipheralblood	blood
5	chrX:75539000-75540400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chrX:75539000-75540600	Enhancers	Primary T helper cells PMA-I stimulated	--
7	chrX:75539000-75540600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chrX:75539200-75539800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
9	chrX:75539200-75540000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chrX:75539200-75540400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
11	chrX:75539200-75540600	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chrX:75539400-75540400	Enhancers	Primary T killer memory cells from peripheral blood	blood
13	chrX:75548400-75549200	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chrX:75548600-75549000	Active TSS	H9 Cell Line	embryonic stem cell
15	chrX:75548800-75549200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
16	chrX:75584400-75584800	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chrX:75585800-75587600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chrX:75587400-75587800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
19	chrX:75587600-75587800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chrX:75646800-75649800	Active TSS	Brain Anterior Caudate	brain
21	chrX:75647000-75647200	Enhancers	Right Ventricle	heart
22	chrX:75647000-75647400	Enhancers	Brain Substantia Nigra	brain
23	chrX:75647200-75647400	Enhancers	Brain Angular Gyrus	brain
24	chrX:75647200-75647400	Enhancers	Brain Cingulate Gyrus	brain
25	chrX:75647200-75647600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chrX:75647200-75647800	Enhancers	Dnd41	blood
27	chrX:75647200-75649000	Active TSS	Brain Hippocampus Middle	brain
28	chrX:75647200-75649400	Active TSS	Brain Inferior Temporal Lobe	brain
29	chrX:75647200-75649400	Active TSS	Stomach Smooth Muscle	stomach
30	chrX:75647400-75647600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chrX:75647400-75647600	Enhancers	Primary T helper cells PMA-I stimulated	--
32	chrX:75647400-75647800	Enhancers	Primary B cells from cord blood	blood
33	chrX:75647400-75647800	Enhancers	Primary T helper cells fromperipheralblood	blood
34	chrX:75647400-75647800	Enhancers	HepG2	liver
35	chrX:75647400-75648000	Enhancers	Primary B cells from peripheral blood	blood
36	chrX:75647400-75648000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chrX:75647400-75648000	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chrX:75647400-75648000	Enhancers	Primary T killer memory cells from peripheral blood	blood
39	chrX:75647400-75650000	Active TSS	Brain Angular Gyrus	brain
40	chrX:75647400-75650600	Active TSS	Brain Cingulate Gyrus	brain
41	chrX:75647600-75647800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
42	chrX:75647600-75647800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chrX:75647600-75647800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chrX:75647600-75647800	Enhancers	Adipose Nuclei	Adipose
45	chrX:75647600-75647800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
46	chrX:75647600-75648000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chrX:75647600-75648000	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chrX:75647600-75648000	Enhancers	Primary T cells fromperipheralblood	blood
49	chrX:75647600-75648000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chrX:75647600-75648000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--

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